Hearing Loss Disease Portal


 
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Most Common: Hearing Loss (D034381), Deafness (D003638), Sensorineural HL (D006319), Waardenburg Syndrome, Usher Syndromes
Disease Browser
Parent Node:
expandMusculoskeletal Abnormalities (D009139)
Parent Node:
expandThoracic Outlet Syndrome (D013901)
..Starting node
..expandCervical Rib Syndrome (D002573)

       Child Nodes:
........expandRuzicka Goerz Anton syndrome (C537192)



 Sister Nodes: 
..expandCervical Rib Syndrome (D002573) Child1
   

Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
Term ID:1990
Name:Cervical Rib Syndrome
Definition:A condition associated with compression of the BRACHIAL PLEXUS; SUBCLAVIAN ARTERY; and SUBCLAVIAN VEIN at the thoracic outlet and caused by a complete or incomplete anomalous CERVICAL RIB or fascial band connecting the tip of a cervical rib with the first thoracic rib. Clinical manifestations may include pain in the neck and shoulder which radiates into the upper extremity, PARESIS or PARALYSIS of brachial plexus innervated muscles; sensory loss; PARESTHESIAS; ISCHEMIA; and EDEMA. (Adams et al., Principles of Neurology, 6th ed, p214)
Alternative IDs:
ParentIDs:MESH:D009139|MESH:D013901
TreeNumbers:C10.668.829.550.850.200 |C14.907.863.200 |C16.131.621.174
Synonyms:Anomalous Cervical Rib Syndrome |Cervical Rib Cervical Band Syndrome |Cervical-Rib-Cervical-Band Syndrome |Cervical Rib Syndromes |Naffziger's Syndrome |Naffziger's Syndromes |Naffziger Syndrome |Naffziger Syndromes |Syndrome, Cervical Rib |Syndrome, Cervical-Rib
Slim Mappings:Cardiovascular disease|Congenital abnormality|Nervous system disease
Reference: MedGen: D002573
MeSH: D002573
OMIM:

Genes:
Phenotypes
Disease Causing ClinVar Variants